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Dagan Jenkins

Showing results (21-30 of 34) with videos related to

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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 3, 2006
Mutation analyses of Uroplakin II in children with renal tract malformationsDagan Jenkins, Maria Bitner-Glindzicz, Sue Malcolm, et al.
Human Molecular Genetics|April 11, 2018
SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20Dale Bryant, Yang Liu, Sanchari Datta, et al.
Journal of the American Society of Nephrology : JASN|May 13, 2005
De novo Uroplakin IIIa heterozygous mutations cause human renal adysplasia leading to severe kidney failureDagan Jenkins, Maria Bitner-Glindzicz, Sue Malcolm, et al.
Journal of Pediatric Urology|May 4, 2007
Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1beta in persistent cloaca and associated kidney malformationsDagan Jenkins, Maria Bitner-Glindzicz, Louise Thomasson, et al.
Cells|November 24, 2023
De-Suppression of Mesenchymal Cell Identities and Variable Phenotypic Outcomes Associated with Knockout of <i>Bbs1</i>Grace Mercedes Freke, Tiago Martins, Rosalind Jane Davies, et al.
American Journal of Human Genetics|October 16, 2012
Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralizationStephen R F Twigg, Deborah Lloyd, Dagan Jenkins, et al.
Nature Genetics|November 19, 2013
Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndromeSérgio B Sousa, Dagan Jenkins, Estelle Chanudet, et al.
American Journal of Human Genetics|May 16, 2007
RAB23 mutations in Carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesityDagan Jenkins, Dominik Seelow, Fernanda S Jehee, et al.
Nature Genetics|January 25, 2011
Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndromeCaroline Rooryck, Anna Diaz-Font, Daniel P S Osborn, et al.
Scientific Reports|August 15, 2020
Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutationsDale Bryant, Marian Seda, Emma Peskett, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 3, 2006
Mutation analyses of Uroplakin II in children with renal tract malformationsDagan Jenkins, Maria Bitner-Glindzicz, Sue Malcolm, et al.
Human Molecular Genetics|April 11, 2018
SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20Dale Bryant, Yang Liu, Sanchari Datta, et al.
Journal of the American Society of Nephrology : JASN|May 13, 2005
De novo Uroplakin IIIa heterozygous mutations cause human renal adysplasia leading to severe kidney failureDagan Jenkins, Maria Bitner-Glindzicz, Sue Malcolm, et al.
Journal of Pediatric Urology|May 4, 2007
Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1beta in persistent cloaca and associated kidney malformationsDagan Jenkins, Maria Bitner-Glindzicz, Louise Thomasson, et al.
Cells|November 24, 2023
De-Suppression of Mesenchymal Cell Identities and Variable Phenotypic Outcomes Associated with Knockout of <i>Bbs1</i>Grace Mercedes Freke, Tiago Martins, Rosalind Jane Davies, et al.
American Journal of Human Genetics|October 16, 2012
Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralizationStephen R F Twigg, Deborah Lloyd, Dagan Jenkins, et al.
Nature Genetics|November 19, 2013
Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndromeSérgio B Sousa, Dagan Jenkins, Estelle Chanudet, et al.
American Journal of Human Genetics|May 16, 2007
RAB23 mutations in Carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesityDagan Jenkins, Dominik Seelow, Fernanda S Jehee, et al.
Nature Genetics|January 25, 2011
Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndromeCaroline Rooryck, Anna Diaz-Font, Daniel P S Osborn, et al.
Scientific Reports|August 15, 2020
Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutationsDale Bryant, Marian Seda, Emma Peskett, et al.
Pageof 4